Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs36208070
F7
1.000 0.040 13 113105519 upstream gene variant -/CCTATATCCT ins 1
rs3045215 0.882 0.040 1 234605171 3 prime UTR variant -/GTTACAATA;GTTATAATA delins 3
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs133049 0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs8089 0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3
rs12115090 0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs181317402 0.925 0.080 19 18896591 5 prime UTR variant A/C snv 2.1E-03 3
rs3093105 0.925 0.080 19 15897578 missense variant A/C snv 0.16 0.18 2
rs762642 1.000 0.040 14 53956335 splice region variant A/C snv 0.35 2
rs2596551 1.000 0.040 6 31364462 upstream gene variant A/C snv 0.16 1
rs3734526 1.000 0.040 6 25779508 3 prime UTR variant A/C snv 6.1E-02 1
rs525380 1.000 0.040 1 20082881 intron variant A/C snv 0.55 1
rs9283880 1.000 0.040 6 27747464 intergenic variant A/C snv 0.34 1
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19